Tag | Content |
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EnhancerAtlas ID | HS145-12253 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:26231550-26232430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr2:26231550-26231562 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr2:26231554-26231566 | AAACAAACAAAC | - | 6.32 | TP53 | MA0106.3 | chr2:26231909-26231927 | GACAAGCCAGGGCTTGCT | - | 6.15 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_09566 | chr2:26230391-26233253 | CD14 | SE_26712 | chr2:26230608-26232892 | Esophagus | SE_28420 | chr2:26231425-26232647 | Fetal_Intestine | SE_29154 | chr2:26231420-26232678 | Fetal_Intestine_Large | SE_32014 | chr2:26231685-26232630 | Gastric | SE_35193 | chr2:26230790-26233105 | HeLa | SE_36382 | chr2:26230622-26233114 | HMEC | SE_64640 | chr2:26230706-26232972 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I026007 | chr2 | 26230471 | 26233268 |
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Enhancer Sequence | AAACAAACAA ACAAACAAAA AGACACCACA TACAGGAATA AAATGTACTG AGGAGACAAA 60 AGAGTGTCAA CCCAAGGATC TCTTTCAGAG GGGTTCCCTT AACTCTGGCA GGCCATGAGG 120 ATGATGCCTG GGAGCCCCAG GATTCTCCTG TTACTTTCTT GTGTCCTCAG AAACCACCCT 180 GGTGACTCAG TAACACAAAC CTAGGGTGTT GAGTGGGTGG GGCACCGCTT CCCACCCCAG 240 TTTATCTGGT TTTCCCAGGC AGAATAGTAC ACTGAAGCTG TAGGCAAAGA GGAAGCCCAA 300 GATAGGGGAA GGCCAGGGTG TTGGTTCCTC AGTTTGTTGA AATCAGAGTC ATGAAGCAAG 360 ACAAGCCAGG GCTTGCTCAG CATTTCTCCT TCCTGGCATG GGTTCACCTC AGCCCCAATT 420 CAGTGGCAGC TCTGTTGGTT CAGAGGGGTG AGGTATCCAA GAGGAGGAAG CTTGTACAAT 480 CCTGCTAGCA GGGGAGGGCT GATGGTAGGG TGGAGTTTCA AAGGAAGCCT CTGACATCTG 540 ACAAAGGCTG AGTCAGTTAT ATTGCCCCAT CTCTGAATCT GGCTTCTCCT GCTCCTCTAC 600 CCTACCCATC CTGCCTTCCA GACACACCAA AGTTCTTTTT ATCCCTGACC ATGACAGGCA 660 TGGCTGCTGT GTGCAGCTTC ATAGGTTGTG CACTGCACAG TTCCAGGAGG TGCTATTCCC 720 ATAGACAAAG GAGTGAATAA CAACTCCAAG AATCATGCAC AATTGTACCA GGCAGCCCCG 780 AGCCAAGCCC TTTTATGACT TCCTTCCTTT CCACATATTG CTTCCCCTGC CACAACTGCC 840 CTTGTTTGCC TTTCCTCCCC CCATTTCTTT ATATGGTGCA 880
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